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3 Records found.
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1.
Schulte, E.C. et al.: Rare variants in β-Amyloid Precursor Protein (APP) and Parkinson's disease. Eur. J. Hum. Genet. 23, 1328-1333 (2015)
2.
van der Zee, J.* et al.: Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration. Acta Neuropathol. 128, 397-410 (2014)
3.
Zech, M. et al.: Niemann-pick C disease gene mutations and age-related neurodegenerative disorders. PLoS ONE 8:e82879 (2013)